|
ENST00000496514.6:c.1636T>G
MANE Select
|
ENSP00000420295.1:p.Ser546Ala
|
|
|
ENST00000255622.10:c.1636T>G
|
ENSP00000255622.6:p.Ser546Ala
|
|
|
ENST00000429163.6:c.799T>G
|
ENSP00000406334.2:p.Ser267Ala
|
|
|
ENST00000496514.5:c.1636T>G
|
ENSP00000420295.1:p.Ser546Ala
|
|
|
NM_000283.3:c.1636T>G
|
NP_000274.2:p.Ser546Ala
|
|
|
NM_001145291.1:c.1636T>G
|
NP_001138763.1:p.Ser546Ala
|
|
|
NM_001145292.1:c.799T>G
|
NP_001138764.1:p.Ser267Ala
|
|
|
XM_011513473.1:c.1855T>G
|
XP_011511775.1:p.Ser619Ala
|
|
|
XM_011513474.1:c.1855T>G
|
XP_011511776.1:p.Ser619Ala
|
|
|
XM_011513475.1:c.1636T>G
|
XP_011511777.1:p.Ser546Ala
|
|
|
XM_011513476.1:c.1855T>G
|
XP_011511778.1:p.Ser619Ala
|
|
|
XM_011513477.1:c.841T>G
|
XP_011511779.1:p.Ser281Ala
|
|
|
XM_011513478.1:c.565T>G
|
XP_011511780.1:p.Ser189Ala
|
|
|
XR_925029.1:n.388A>C
|
|
|
|
NM_001350154.1:c.799T>G
|
NP_001337083.1:p.Ser267Ala
|
|
|
NM_001350155.1:c.481T>G
|
NP_001337084.1:p.Ser161Ala
|
|
|
XM_011513473.3:c.1855T>G
|
XP_011511775.1:p.Ser619Ala
|
|
|
XM_011513474.3:c.1855T>G
|
XP_011511776.1:p.Ser619Ala
|
|
|
XM_011513475.2:c.1636T>G
|
XP_011511777.1:p.Ser546Ala
|
|
|
XM_011513476.3:c.1855T>G
|
XP_011511778.1:p.Ser619Ala
|
|
|
XM_011513478.2:c.565T>G
|
XP_011511780.1:p.Ser189Ala
|
|
|
XM_017008284.1:c.799T>G
|
XP_016863773.1:p.Ser267Ala
|
|
|
XM_017008285.1:c.799T>G
|
XP_016863774.1:p.Ser267Ala
|
|
|
XM_017008286.1:c.799T>G
|
XP_016863775.1:p.Ser267Ala
|
|
|
NM_001350154.2:c.799T>G
|
NP_001337083.1:p.Ser267Ala
|
|
|
NM_001350155.2:c.481T>G
|
NP_001337084.1:p.Ser161Ala
|
|
|
NM_000283.4:c.1636T>G
MANE Select
|
NP_000274.3:p.Ser546Ala
|
|
|
NM_001145291.2:c.1636T>G
|
NP_001138763.2:p.Ser546Ala
|
|
|
NM_001145292.2:c.799T>G
|
NP_001138764.2:p.Ser267Ala
|
|
|
NM_001350154.3:c.799T>G
|
NP_001337083.1:p.Ser267Ala
|
|
|
NM_001350155.3:c.481T>G
|
NP_001337084.1:p.Ser161Ala
|
|
|
NM_001379246.1:c.799T>G
|
NP_001366175.1:p.Ser267Ala
|
|
|
NM_001379247.1:c.799T>G
|
NP_001366176.1:p.Ser267Ala
|
|
